A randomized trial of tirilazad mesylate in patients with acute stroke (RANTTAS). The RANTTAS Investigators - PubMed (original) (raw)
Clinical Trial
A randomized trial of tirilazad mesylate in patients with acute stroke (RANTTAS). The RANTTAS Investigators
No authors listed. Stroke. 1996 Sep.
Abstract
Background and purpose: Tirilazad mesylate, a nonglucocorticoid 21-aminosteroid lipid peroxidation inhibitor, has shown promise as a neuroprotectant in experimental models of focal cerebral ischemia.
Methods: To test whether early treatment with tirilazad, 6 mg/kg per day for 3 days, would improve functional outcome after acute human stroke, 27 North American centers conducted a prospective, randomized, double-blinded, vehicle-controlled trial in patients with acute stroke treated within 6 hours of onset. The primary outcome measures were disability as measured by the Glasgow Outcome Scale and activities of daily living by the Barthel Index determined 3 months after stroke.
Results: From May 1993 through December 1994, 660 patients were randomized. The trial was prematurely terminated on the advice of an independent monitoring committee after review of outcome data at a preplanned interim analysis. In 556 fully eligible patients (276 tirilazad, 280 vehicle), the odds ratio of a favorable outcome in favor of tirilazad was 0.87 (95% confidence interval [CI], 0.60 to 1.25) for the Glasgow Outcome Scale and 0.87 (95% CI, 0.60 to 1.25) for the Barthel Index, after adjustment for imbalances between the groups in preexisting disability, prior stroke, and diabetes.
Conclusions: These observations suggest that tirilazad, 6 mg/kg per day for 3 days administered beginning at a median of 4.3 hours after stroke, does not improve overall functional outcome.
Comment in
- High-dose tirilazad for acute stroke (RANTTAS II). RANTTAS II Investigators.
Haley EC Jr. Haley EC Jr. Stroke. 1998 Jun;29(6):1256-7. Stroke. 1998. PMID: 9626304 Clinical Trial. No abstract available.
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